FDA applicant

Cybercare Technologies, Inc.

Atlanta, GA3 decisions2000–20010 recalls

FDA records 3 decisions for Cybercare Technologies, Inc. (Atlanta, GA) from 2000 to 2001: 3 510(k) clearances. Most are in product codes DQD (Stethoscope, Electronic) and CGA (Glucose Oxidase, Glucose). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Cybercare Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cybercare Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Cybercare Technologies, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Cybercare”

FDA records each applicant name separately; these may or may not be the same firm.

Cybercare, Inc. 2

Cybercare Technologies, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Cybercare”